Recovery of Phosphorus from Hypophosphite-Laden Wastewater: A Single-Compartment Photoelectrocatalytic Cell System Integrating Oxidation and Precipitation

次磷酸 化学 激进的 双功能 废水 阴极 无机化学 流出物 降水 化学工程 核化学 废物管理 催化作用 有机化学 物理 气象学 工程类 物理化学
作者
Juanjuan Zhang,Xu Zhao,Yan Wang,Ridha Djellabi‬‬‬‬‬‬‬‬
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:54 (2): 1204-1213 被引量:37
标识
DOI:10.1021/acs.est.9b05125
摘要

Recovery of phosphorus through precipitation from hypophosphite-laden wastewater is more difficult than from orthophosphate-laden wastewater because of the higher solubility of hypophosphite (H2PO2–). Herein, a single-compartment photoelectrocatalytic (PEC) cell system consisting of a TiO2/Ni–Sb–SnO2 bifunctional photoanode and an activated carbon fiber (ACF) cathode with dosing Fe2+ ions was developed for recovery of phosphorus in the form of FePO4 from hypophosphite-laden wastewater. In the PEC process, H2PO2– with an initial concentration of 1.0 mM was completely oxidized and recovered within 30 min at 3.0 V, and the pseudo-first-order rate constant of H2PO2– oxidation was ∼4 times than that in the electrocatalytic process and even ∼89 times than that in the photocatalytic process. The bifunctional photoanode can simultaneously generate •OH radicals and O3; the ACF cathode can electrogenerate H2O2; H2O2, O3, and the added Fe2+ can interact with each other to produce •OH radicals and Fe3+ ions. •OH radicals mainly from the Fenton process were responsible for oxidation of H2PO2– to PO43–, which immediately combined with Fe3+ to form FePO4 at the optimized conditions to realize recovery of phosphorus. The long-term stability of this system was demonstrated. The efficiency for actual electroless nickel plating effluents was exhibited.
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